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Angular non-critical phase-matching second-harmonic-generation characteristics of RECOB (RE = Tm, Y, Gd, Sm, Nd and La) crystals

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Abstract

For the first time, the angular non-critical phase-matching (A-NCPM) second-harmonic-generation (SHG) characteristics of a family of monoclinic oxoborate crystals, RECa4O(BO3)3 (RECOB, RE = Tm, Y, Gd, Sm, Nd and La), were comprehensively investigated. For all of the realizable A-NCPM SHG styles, the feature parameters including PM wavelength, angular, wavelength and temperature acceptance bandwidths, have been derived from the theory and verified by the experiments. We discovered that the closer the ion radius between RE3+ and Ca2+, the smaller the birefringence, and the better the A-NCPM SHG properties. As a result, for the Type-I SHG on Y-axis which has the largest effective nonlinear optical coefficient (deff) among the three realizable A-NCPM styles, NdCOB crystal presents the longest PM wavelength (927 nm), the largest angular acceptance bandwidth (Δθ⋅l1/2 = 84.3 mrad·cm1/2, Δϕ⋅l1/2 = 58.8 mrad·cm1/2), and the broadest wavelength acceptance bandwidth (8.7 nm). This discovery will contribute to the design of new NCPM materials, at the same time the parameter formula will be helpful for the theoretical prediction of NCPM performance.

© 2017 Optical Society of America

1. Introduction

At present, visible lasers have been applied to many fields, including laser display, medicine, optical storage, bio-photonics, undersea communication, marking and precision micro fabrications etc [1–4]. Based on the phase-matching (PM) technology of nonlinear optical (NLO) crystals, the frequency doubling (i.e. SHG) of near-infrared lasers has been an efficient and convenient approach to obtain such sources with high beam quality and reliability [5–7]. Among all of the PM configurations, the ones which propagate along the optical principal axes of the NLO crystal are very special, which are also known as angular non-critical phase-matching (A-NCPM) [8,9]. The A-NCPM possesses two distinctive advantages, i.e. the large angular acceptance bandwidth and the absence of the beam walk-off, so it is considered to be the optimal PM style. Therefore, in this condition long crystal can be utilized to increase the frequency conversion efficiency [10–15]. On the whole, the A-NCPM is rare and precious, since the fact that the refractive indexes of NLO crystals are usually unchangeable, which makes the A-NCPM wavelengths are almost fixed and limited. Such situation applies to most of the bulk NLO crystals, including the well-known KH2PO4 (KDP), KTiOPO4 (KTP), BaB2O4 (BBO), and BiB3O6 (BIBO) [12]. By time now, the most popular A-NCPM NLO crystal is LiB3O5 (LBO), whose refractive indexes sensitively change with the temperature. On X-axis it can realize type-I SHG, the A-NCPM SHG wavelength range is 0.94~1.65 µm when the temperature varied in the range of −10~300 °C, and the effective NLO coefficient deff is 0.85 pm/V (d32). On Z-axis LBO can realize type-II SHG, the NCPM wavelength range is 1.12~1.46 µm when the temperature varied in −50~50 °C, and the deff is 0.67 pm/V (d31) [12]. Beside the temperature-dependence, the component dependence is another means to realize broad waveband A-NCPM. In 1999, Furuya et al. found that the ratio of lattice constants (a/b and a/c) for GdxY1-xCOB crystals change linearly with the compositional parameter x. These results confirmed that GdxY1-xCOB was a substitutional solid solution, and its refractive indices as well as A-NCPM wavelength could be continuously adjusted by varying the parameter x [10,16,17]. Subsequently, similar properties are also observed in other series of mixed RECOB crystals, such as LuxGd1-xCOB and ScxGd1-xCOB [8,18]. Comparing to the 0.94~1.65 µm A-NCPM SHG of LBO crystal, RECOB type crystals (where RE denotes a rare-earth element like Tm, Y, Gd, La, etc. or their “mixture”) can extend the PM wavelength toward short wave direction, which covers the work waveband of Ti:Sapphire lasers and near infrared laser diodes, i.e. 0.7~0.9 µm. Now, the A-NCPM frequency conversion has been one of the representative NLO applications of RECOB type crystals. Nevertheless, the related researches are still separated and scattered, the internal connection among different RECOB crystals has never been explored. Corresponding, the A-NCPM feature parameters, whether they are the experimental values in most cases or the theoretical calculated values in a few cases, have never been comprehensively investigated and compared.

In this paper, the A-NCPM SHG characteristics of RECOB (RE = Tm, Y, Gd, Sm, Nd and La) crystals are intensively studied. The single crystal growth, transmission spectra, orientation determination and refractive indices are shown in parts 2 to 5, as the necessary preparatory information. In parts 6 to 10, we discussed five A-NCPM SHG properties respectively, including the realizable styles, PM wavelength, angular acceptance, wavelength acceptance, and temperature acceptance. For the first time, the Sellmeier equations as well as the A-NCPM SHG properties of SmCOB, NdCOB crystals are reported. For the other four crystals, TmCOB, YCOB, GdCOB and LaCOB, the parameters presented in parts 2 to 7 are cited from the previous literatures which have been marked out in the text, and the experimental as well as the theoretical data in parts 8~10 are newly obtained in this work.

It should be noted that although NCPM technology include other manners like wavelength NCPM, temperature NCPM, we only concerned A-NCPM here. For simplicity, we use “NCPM” instead of “A-NCPM” in the followed parts.

2. Single crystal growth

Before Czochralski single crystal growth, the polycrystalline RECOB raw materials were prepared from high purity (4N) CaCO3, Re2O3 (RE = Tm, Y, Gd, Sm, Nd and La) and H3BO3 powders. They were weighed referring to their nominal compositions. Considering the evaporation of B2O3 component during the solid-state reaction and crystal growth, an excess quantity of H3BO3 (1~4% in mass ratio) were added to the starting materials. After mixing the starting materials completely, the first calcination was carried out up to 950~1000 °C for 10~20 hours to decompose the H3BO3 and CaCO3. Then the calcined powders were ground, remixed and pressed into tablets. Polycrystalline RECOB components were finally obtained by the second calcination at 1100~1200 °C for 15~25 hours. In order to make the components homogeneous enough for single crystal growth, the RECOB melts were kept 30~50 °C higher than their melting points (the melting points for different RECOB crystals are varied from 1390°C to1520 °C) for more than 12 hours. More crystal growth details can be found in previous reports [19–25]. We found that the TmCOB and LaCOB crystals were more difficult to grow comparing to other four RECOB (RE = Y, Gd, Sm and Nd) crystals. The LaCOB crystal is easy to crack, due to the approximate cleavage along the (2¯01) planes, so its growth procedure needs to be carried out blandly. Different to the LaCOB crystals, the growth difficulty of the TmCOB crystals was induced by the narrow congruent region of TmCOB crystal. It was found that the deficient H3BO3 (excess amount < 3.0 wt%) or over added H3BO3 (excess amount > 4 wt%) would be harmful to high-quality TmCOB single crystals. Figure 1 shows the as-grown RECOB crystals that we have obtained. As the material basis of this paper, it can be seen that integrally they have large size and high optical quality. Similarly, the large size substitutional solid solutions with different RE components (hereafter we denote as “the mixed crystals”) can also be achieved by the Czochralski method, including GdxY1-xCOB [16], NdxY1-xCOB [26], NdxGd1-xCOB [27], NdxLa1-xCOB [28], and SmxY1-xCOB [29].

 figure: Fig. 1

Fig. 1 As-grown RECOB crystals (RE = Tm, Y, Gd, Sm, Nd and La).

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3. Transmission spectra

With a NIR-UV-VIS spectrophotometer (U-4001, Hitachi), the optical transmission spectra of RECOB type crystals were recorded at room temperature. All the samples were prepared along the <010> direction and were mechanical polished with a thickness of ~2 mm. The measuring scope was 190~1600 nm, and the scanning step was 1 nm. Figure 2 presents the optical transmission spectra of TmCOB, SmCOB and NdCOB crystals. Among the concerned RECOB (RE = Tm, Y, Gd, Sm, Nd and La) crystals, YCOB, GdCOB and LaCOB are colourless and transparent, which have no absorption peaks at 210~2500 nm, 320~2700 nm and 200~2400 nm, respectively [20,30,31]. The corresponding mixed crystals, GdxY1-xCOB, LaxGd1-xCOB and LaxY1-xCOB are also colourless and transparent without absorption peak from ultra-violet (UV) to near infrared. The other three crystals, TmCOB, SmCOB and NdCOB, exhibit different colours, as shown in Fig. 1. They are relevant to different absorption peaks in visible waveband, as presented in Fig. 2. Such absorption characteristics are also inherited by the mixed crystals derived from them, like SmxY1-xCOB and NdxGd1-xCOB. The location and the width of the absorption peaks are almost the same, but the peak intensities will be obviously weaker, compared with SmCOB and NdCOB crystals. In Fig. 2, it is found that SmCOB exhibits less absorption peaks in visible region than TmCOB and NdCOB, with transmittance higher than 70% at 366~398 nm and 421~1054 nm. It means that SmCOB possesses wider spectral selecting space than TmCOB and NdCOB in NLO applications. The existence of absorption peaks in visible region for TmCOB, SmCOB, NdCOB and their derivative mixed crystals will affect their NLO applications more or less.

 figure: Fig. 2

Fig. 2 Transmission spectra of several colored RECOB crystals.

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4. Crystal orientation

The determination of crystal orientation is the first step for investigating the NLO properties of RECOB crystals, which will directly affect the followed measurement of refractive indices and the calculation of NCPM characteristics. RECOB crystals are monoclinic biaxial materials which belong to the point group m. They possess three orthogonal optical principal axes X, Y and Z, among which the Y axis is reversed with the two-folded crystallographic axis b, and the other two axes X and Z locate in (010) plane which are respectively close to the crystallographic axes c and a with certain angles, as shown in Fig. 3. Consistent with the tradition, the X, Y, Z axes are assigned according to the relation for the principal refractive indices nX < nY < nZ. The RECOB crystals are prone to grow along b axis, and their (2¯01), (010) and (101) crystallographic planes are usually exposed in this situation, which can help us for crystal orientation and sample preparation.

 figure: Fig. 3

Fig. 3 Relationships between the crystallographic axes (a, b and c) and the optical principal axes (X, Y and Z) for RECOB crystals.

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The crystal orientation of TmCOB, YCOB, GdCOB and LaCOB had been reported previously, here we newly determined the values of SmCOB and NdCOB by using of the polarized microscopy (Axio Lab. A1, ZEISS), and all of the results were summarized in Table 1. Based on the orientation of RECOB crystals, the relationships between the crystallographic axes (a and c) and optical principal axes (Z and X) were found to be 23.5~27.8° for (a, Z) and 12.4~16.5° for (c, X), respectively. The angle β between the crystallographic axes a and c for all of the crystals unchanged basically, which was 101.2 ± 0.2°, as shown in Table 1. The light source used in this measurement is a He-Ne laser (632.8 nm). Because no dielectric frame rotation has ever been observed in such crystals [32,34], the data in Table 1 will be available for other wavelengths, either.

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Table 1. Crystal orientation of RECOB crystals

5. Refractive index

RECOB crystals are optical biaxial crystals, and each crystal needs to be processed into two right angle prisms whose ridges are along different optical principal axes, to permit the measurement of X, Y and Z polarization light, respectively. Utilizing a full-automatic, high-precision (2 × 10−6) refractive-index measurement instrument (Spectro Master @HR, Trioptics), the refractive indices of SmCOB, NdCOB, LaCOB crystals were measured, and the results were exhibited in Fig. 4. The refractive index data were obtained by fitting the dispersion curves according to the followed Sellmeier equations

ni2=Ai+Biλ2CiDiλ2(i=X,Y,Z)
where λ is the wavelength in micrometers, and Ai, Bi, Ci and Di are Sellmeier parameters for each principal axis. Table 2 presents the Sellmeier parameters which give the best fits for the measured data in Fig. 4. The solid lines in Fig. 4 are the fitted refractive-index dispersion curves with the least square method. It can be seen that they are in good agreement with the experimental data. The accuracy of these Sellmeier equations is further confirmed by the NCPM SHG experiments, which is reported in the part 7.1 of this paper. The Sellmeier coefficients for TmCOB, YCOB and GdCOB crystals come from the previous reports [13,35], which are also listed in Table 2. We calculated the birefringence of these crystals at 1064 nm, and found that among the mentioned RECOB crystals, TmCOB possessed the largest birefringence (0.0425) while NdCOB showed the smallest birefringence (0.0279).

 figure: Fig. 4

Fig. 4 Refractive-index dispersion curves of several RECOB crystals.

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Tables Icon

Table 2. Sellmeier equation coefficients of RECOB crystals

6. NCPM SHG style

For biaxial NLO crystals, NCPM is the PM direction along the optical principal axes. RECOB crystals have three optical principal axes X, Y and Z, and each axis has two types of SHG PM styles, i.e. ssf (type-I) and sff (type-II), so in the ideal case they can have six NCPM SHG wavelengths at least. In view of the point group m and the Kleimann symmetry, the contracted matrix of nonlinear coefficients of RECOB crystals can be expressed as

d11d12d13000d31d32d330d310d320d120d130
According to the expressions of deff in principal planes [36], the deff on each optical principal axis can be determined, as shown in Table 3. For type-I NCPM on X axis and type-II NCPM on Z axis, the deff is found to be zero, which indicates that they have no practical value, so we only need to consider the other four NCPM styles. Many researches have manifested that the independent NLO coefficients dij among different RECOB crystals are approximately equal within the experimental uncertainty [13,36–40]. Here we selected the dij values of GdCOB crystal [37] as the representatives, and listed them in the parentheses of Table 3. Although the deff of type-II NCPM on X axis is the largest (1.67 pm/V), the theoretical calculations from refractive-index equations indicates that the type-II NCPM on X axis is unrealizable [20]. For verifications, we have scanned multiple RECOB crystals with an optical parametric oscillator (OPO) laser, and no type-II NCPM was found on their X axes during the wavelength tuning range of 0.4~2.4 µm. So practically there are only three realizable NCPM styles for RECOB type crystals, i.e. type-I, type-II NCPM on Y axis, and type-I NCPM on Z axis.

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Table 3. The effective nonlinear optical coefficients deff of RECOB type crystals along different optical principal axes. The values of the NLO coefficients came from Reference [37].

From the viewpoint of NLO coefficient, the type-I NCPM on Y axis which has the largest deff of 0.60 pm/V should be the most favourable. It is close to the deff values of LBO crystal, i.e. 0.85 pm/V for type-I NCPM and 0.67 pm/V for type-II NCPM. Besides, the type-I NCPM on Y axis also has special material advantage, because RECOB crystals are easy to grow along the crystallography b axis which is collinear with the Y optical axis, so it is convenient to obtain long Y-cut samples to perform high efficiency NCPM SHG frequency conversions.

7. NCPM SHG wavelength

7.1 Calculation and experimental measurement

Using the Sellmeier equation parameters listed in Table 2, the NCPM SHG wavelengths of RECOB (Re = Tm, Y, Gd, Sm, Nd and La) crystals were calculated, and the results for practical NCPM styles, i.e. type-I and type-II on Y axis, and type-I on Z axis, were shown in Table 4. In order to examine these values, Y- and Z-cut RECOB samples were processed for experimental measurements. An OPO (Opolette HE 355 II) tunable laser was used as the fundamental laser source (410~2400 nm). The output light was linearly polarized along the vertical direction. The laser pulse width was about 5 ns and the repetition rate was 20 Hz. The average output power depended on the work wavelength and driving current, which varied in the range of 0~12 mW. For Y-cut RECOB crystal samples, the polarization of the Y-transmitted fundamental wave was along the Z-axis for type-I NCPM SHG (i.e. slow wave polarization), but along the angle bisector of Z-axis and X-axis for type-II NCPM SHG (i.e. slow wave polarization plus fast wave polarization). For Z-cut RECOB crystal samples, the polarization of the Z-transmitted fundamental wave was along the Y-axis for type-I NCPM SHG (i.e. slow wave polarization). When the transmitting direction and polarization state of the fundamental wave was correctly arranged, the accurate NCPM SHG wavelength could be determined by tuning the output wavelength of the OPO laser to find which one yielded the maximum SHG output signal. The NCPM SHG wavelengths for different RECOB crystals were measured and listed in Table 4.

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Table 4. Calculated and measured NCPM SHG wavelength of RECOB crystals

In this study, the type-II NCPM SHG wavelengths on Y-axis for SmCOB and NdCOB crystals didn’t obtained, which might attribute to the low output power at the infrared waveband of the OPO laser, and the strong absorption of fundamental wave around 1.4 µm for SmCOB, as well as the strong absorption of SHG wave around 0.8 µm for NdCOB, as shown in Fig. 2. By comparing the calculated results with the measured results in Table 4, it can be concluded that the Sellmeier equations of SmCOB, NdCOB, and LaCOB crystal which we reported in this paper are quite accurate. The discrepancies between the calculated data and the experimental values are less than 10 nm, and in some conditions they are only 2 nm. At the same time, for the other three crystals TmCOB, YCOB and GdCOB the wavelength discrepancies between calculations and experiments are also satisfactory basically, which reflects the accuracy of the corresponding Sellmeier equations. The largest difference comes from the type-II NCPM on Y-axis of GdCOB crystal, which is found to be 50 nm. Generally, for type-I NCPM SHG wavelengths the experimental values are found to agree well with the calculated ones, while for the type-II NCPM SHG wavelengths the errors are more obvious which can reach several tens of nanometers. The main reason for this phenomenon is that for type-II PM there are three different refractive indexes (slow fundamental wave, fast fundamental wave and fast SHG wave) which participate the calculation of PM wavelength, while for type-I PM only two different refractive indexes participate the calculation (slow fundamental wave and fast SHG wave), so the precise prediction of type-II PM property proposes higher requirement for the accuracy of Sellmeier equations. In addition, the environmental temperature discrepancy between the refractive index measurements and the NCPM SHG experiments will also cause the wavelength deviations between calculation and measurement.

For multiple components RECOB, i.e. mixed RECOB crystals, the NCPM wavelength can be adjusted continuously by varying the component parameter x. Taking SmxY1-xCOB series crystals for example, Table 4 indicates that theoretically the type-I and type-II NCPM SHG wavelengths adjusting ranges on Y-axis are 723~903 nm and 1023~1390 nm, respectively, and the type-I NCPM wavelength adjusting range on Z-axis is 827~1123 nm. It means the spectral range from 0.72 to 1.39 µm can be absolutely covered by SmxY1-xCOB crystals.

7.2 Influence of rare earth ions RE3+

For single component and mixed RECOB crystals, the difference of rare earth ions RE3+ leads to the variation of optical properties, including the transmission spectrum, the orientation of the optical principle axis, and the refractive index. Accordingly, the refractive index dispersion decides the NCPM SHG wavelength directly. So it is necessary to explore the relationships among the type of RE3+ ions, the refractive index, and the NCPM SHG wavelength. A theoretical analysis indicates that the NCPM SHG wavelength takes on the opposite change trend with the birefringence of the fundamental wave, which is proved in the first part of Appendix (12.1) in details. In Figs. 5a, 5b and 5c, we plotted the variation of birefringence and NCPM SHG wavelength with rare earth radius for the three available NCPM SHG styles, respectively. Referencing Table 4, we chose 800, 1300 and 1064 nm as the representative fundamental wavelengths for type-I, type-II NCPM SHG on Y-axis and type-I NCPM SHG on Z-axis, respectively. The corresponding birefringence of different RECOB crystals were plotted in Figs. 5a-5c. Because we have not experimentally found the type-II NCPM SHG wavelengths on Y-axes of SmCOB and NdCOB crystals, the calculated data of 1390, 1578 nm for them were used in Fig. 5b. Other NCPM SHG wavelengths in Figs. 5a~5c were adopted with the experimental data in Table 4. For RECOB crystals, the ionic radius of Tm3+, Y3+, Gd3+, Sm3+, Nd3+, La3+ and Ca2+ positive ions are 0.880, 0.890, 0.938, 0.958, 0.983, 1.032 and 0.995 Å, respectively. When the radius of the rare earth ion RE3+ increases, the average bond length perpendicular to the plane of RE-O bond will rapidly increases, either, which weakens the electronegativity of RE element, decreases the crystal melting temperature, increases the crystal lattice stress, and elevates the risk of cracking [21]. The crystal growths have manifested that LaCOB is easier to crack than other five RECOB (Tm, Y, Gd, Sm and Nd) crystals.

 figure: Fig. 5

Fig. 5 Variation of birefringence and NCPM SHG wavelength with rare earth ion radius in RECOB crystals.

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Figures 5a, 5b and 5c exhibit the same variation discipline between the ionic radius of RE3+ and the birefringence, i.e. the closer ion radius of RE3+ and Ca2+, the smaller birefringence. At the same time, the experimental results are accordant with the theoretical derivations of the first part of the appendix (12.1), i.e. the small crystal birefringence corresponds to the long NCPM SHG wavelength. So there is the closer ion radius of RE3+ and Ca2+, the longer NCPM SHG wavelength. In Figs. 5a-5c, NdCOB possesses the smallest birefringence, correspondingly its NCPM SHG wavelengths are the longest, which are 927, 1578 and 1205 nm, respectively. TmCOB possesses the largest birefringence, so its NCPM SHG wavelengths are the shortest, which are 716, 1011 and 815 nm, respectively. As the optimum NCPM style of RECOB type crystals which has the largest deff, the type-I NCPM SHG on Y-axis presents a tuning amplitude larger than 200 nm, as shown in Fig. 5a. With the increase of ionic radius of RE3+, the birefringence decreases from 0.044 to 0.029 and then increases to 0.035, correspondingly, the NCPM SHG wavelength increases from 716 nm to 927 nm and then decreases to 808 nm (Fig. 5a). The type-II NCPM SHG wavelength on Y-axis changes from 1011 nm to 1578 nm and then decreases to 1178 nm with the increase of ion radius of RE3+ (Fig. 5b). The type-I NCPM SHG wavelength on Z-axis changes from 815 nm to 1205 nm and then decreases to 1001 nm (Fig. 5c).

In short, in this part we revealed the NCPM SHG wavelength variation discipline of RECOB crystals for the first time, i.e. it depends on the birefringence. The more essential reason is the radius difference between the rare earth ion RE3+ and the lattice positive ion Ca2+, not the absolute radius of RE3+. The basic principle for crystal design can be summarized as: the closer ion radius between RE3+ and Ca2+, the longer NCPM SHG wavelength.

8. Angular acceptance bandwidth

Besides of deff and PM wavelength, various acceptance bandwidths are also known as the basic attributes of NLO crystal. According to the different influence parameters, the acceptance bandwidths are mainly divided into three categories, i.e. angular, wavelength, and temperature, which relate to the spatial dispersion, frequency dispersion, and temperature dispersion of refractive indexes, respectively. In the followed three parts, we will discuss them one by one, aiming at the NCPM SHG configurations in RECOB crystals. For the angular NCPM SHG concerned in this paper, extremely large angular acceptance bandwidth is one of the most important advantages. Unfortunately, by time now no accurate mathematic expressions of this parameter are reported for NCPM SHG situations, to the best of our knowledge. The main reason is they are related to the second derivative of the wave vector mismatching, which are complicated and difficult to deduce. In the second part of the appendix (12.2), we give a complete theoretical deduction about these expressions for biaxial NLO crystal, and the results are summarized in the Table 8. As we have known it is the first time that the angular acceptance bandwidths of NCPM SHG styles are obtained directly in theory. In the past, people got these parameters only by indirectly experimental measurement. If the condition of nx = ny is substituted in these expressions, the results in Table 8 are also available for uniaxial NLO crystal. Therefore, the deduction and the results of the second part of the appendix (12.2) are meaningful for all of the anisotropic NLO crystals.

Using the expressions in Table 8, we calculated the internal angular acceptance bandwidths for the NCPM SHG of different RECOB crystals, based on the Sellmeier equation coefficients listed in Table 2. Then referencing the sine law of refraction and the refractive indexes of various crystals at their NCPM SHG wavelengths, we obtained the external angular acceptance bandwidths in theory, which were shown in Table 5. As discussed in the part 6, only three NCPM SHG styles are realizable in these crystals, including type-I, type-II on Y axis, and type-I on Z axis. The grey blocks represent unavailable NCPM SHG style (type-II on Z axis), and unavailable angular acceptance bandwidth (Δϕ⋅l1/2 on Z axis). As introduced in the second part of the appendix (12.2), there is only angular acceptance bandwidth of Δθ⋅l1/2, and no Δϕ⋅l1/2 for the NCPM on Z axis. Beside of the theoretical calculation, we also actually measured the angular acceptance bandwidths for type-I NCPM SHG on Y axis, including Δθ⋅l1/2 and Δϕ⋅l1/2, for five RECOB crystals. The external angular tuning curves of the SHG signals are shown in Fig. 6, and the corresponding angular acceptance bandwidths are listed in Table 5. Because TmCOB has severe absorption for its type-I NCPM SHG output on Y axis (358 nm), we cannot accurately measure the variation of SHG signal in this crystal, so the corresponding experimental data of TmCOB crystal are unavailable in Fig. 6 and Table 5. In addition, we measured the angular acceptance bandwidths of type-I NCPM SHG on Z axis, for LaCOB crystal. The results are listed in Table 5 as well. It can be seen that all of the experimental data are in good agreement with the calculated data, with discrepancies less than 5 mrad·cm1/2. It indicates that the theoretical calculation formulas obtained in the second part of the appendix (12.2) are correct, and the refractive index dispersion equations shown in part 5 are precise.

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Table 5. External angular acceptance bandwidth of NCPM SHG in RECOB crystals

 figure: Fig. 6

Fig. 6 External angular tuning curves of the SHG signals in different RECOB crystals, for the type-I NCPM on Y axis.

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From Table 5, we can find the followed disciplines about the external angular acceptance bandwidth of RECOB crystals:

  • (1) The angular acceptance bandwidths of NCPM SHG vary from 40 to 150 mrad·cm1/2. These values are an order of magnitude larger than the data of critical PM, which are 3~5 mrad·cm typically [19,41,42].
  • (2) For Type-I and Type-II SHG on Y axis, the angular acceptance bandwidth in θ direction (Δθ⋅l1/2) is obviously larger than the corresponding value in ϕ direction (Δϕ⋅l1/2).
  • (3) For Type-I SHG on Z axis, the angular acceptance bandwidth in YZ principal plane (ϕ = 90°) is obviously larger than the corresponding value in XZ principal plane (ϕ = 0°).
  • (4) For Type-I NCPM SHG, the angular acceptance bandwidth on Y axis is similar to the corresponding value on Z axis. It is applied to both Δθ⋅l1/2 and Δϕ⋅l1/2.
  • (5) For SHG on Y axis, the angular acceptance bandwidth of Type-I is obviously smaller than the corresponding value of Type-II. It is applied to both Δθ⋅l1/2 and Δϕ⋅l1/2. So, if singly considering the angular acceptance bandwidth, Type-II SHG on Y axis is the most favourable among all of the three realizable NCPM styles.
  • (6) For Type-I SHG on Y-axis which has the largest deff among the three realizable NCPM styles, NdCOB presents the largest angular acceptance bandwidth (Δθ⋅l1/2 = 84.3 mrad·cm1/2, Δϕ⋅l1/2 = 58.8 mrad·cm1/2) among the six RECOB crystals.

9. Wavelength acceptance bandwidth

For various angular NCPM SHG styles, the mathematical expressions of the wavelength acceptance bandwidth Δλ⋅l are discussed in the third part of the appendix (12.3) and the results are summarized in the Table 9. Combining with the Sellmeier equation coefficients listed in Table 2, we calculated Δλ⋅l for the six RECOB (RE = Tm, Y, Gd, Sm, Nd and La) crystals, as shown in Table 6. It can be seen that the Δλ⋅l of type-II NCPM SHG is larger than the values of type-I NCPM. At the same time for type-I NCPM SHG the Δλ⋅l on the Z axis is larger than that on the Y axis. Such discipline can be intuitively explained by the corresponding formula in Table 9, considering the property of BZ > BY, DZ > DY (Table 2). Among all of the six RECOB crystals, the largest Δλ⋅l comes from NdCOB, and the smallest comes from TmCOB, which can attribute to the radius difference between the rare earth ion RE3+ and the lattice positive ion Ca2+. As shown in Fig. 5, the Nd3+ ion radius is the closest to the Ca2+ ion radius, correspondingly the birefringence of NdCOB is the smallest, so the Δλ⋅l is the largest. On the contrary, the Tm3+ ion radius is the farthest to the Ca2+ ion radius, so the birefringence of TmCOB is the largest and the Δλ⋅l is the smallest. For Gd3+ and La3+, their ion radiuses have similar discrepancy to the Ca2+ ion radius, so GdCOB and LaCOB exhibited similar birefringence and wavelength acceptance bandwidth. In summary, the radius difference between Re3+ and Ca2+ is still the decisive factor for the magnitude of wavelength acceptance bandwidth, i.e. the small radius difference corresponds to the small birefringence and large Δλ⋅l.

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Table 6. Wavelength acceptance bandwidth of NCPM SHG in different RECOB crystals

By fixing RECOB crystals at angular NCPM SHG conditions, we measured wavelength tuning curves of the SHG signals, with an OPO laser as the fundamental light sources. Four representative experimental curves were shown in Fig. 7. All of the measured results of the wavelength acceptance bandwidths are presented in Table 6. Limited by the experimental conditions or the crystal’s characteristics, some of the measured values were not available, and the reasons were individually explained as the annotations of the Table 6. It can be seen that the calculated values are in good agreements with those measured from the experiments, which proves the reliability of the theoretical deduced formula in Table 9.

 figure: Fig. 7

Fig. 7 Wavelength tuning curves of the SHG signals in different RECOB crystals, for the type-I SHG on Y axis.

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10. Temperature acceptance bandwidth

A discussion on the temperature acceptance bandwidth for the NCPM SHG of biaxial crystal is given in the fourth part of the appendix (12.4), and the theoretically deduced results are presented in the Table 10. Based on the thermo-optic dispersion formula of YCOB and GdCOB crystals [43,44], the temperature acceptance bandwidth for these two crystals are calculated out, as shown in the Table 7. It can be seen that for Type-I NCPM SHG our calculation values are basically in agreement with the experimental data reported in the references [43,44]. Although there are no measured data about the Type-II NCPM SHG of YCOB and GdCOB crystals, the existing experimental results of Gd0.132Y0.868COB crystal (Y-axis, ω = 1053 nm, ΔTl = 43.5 °C·cm) [45] and La0.1204Y0.8796COB crystal (Y-axis, ω = 1064 nm, ΔTl = 38.4 °C·cm) [46] are close to the calculating values in the Table 7, which can prove the validity of the theoretical deductions. As mentioned in the references [44], the data discrepancy between calculation and experiment may come from three aspects: (1) The thermal rotations of optical indicatrix axes in RECOB type crystals, which have been ignored during the formulae deduction procedures of the Table 10. (2) The crystal-to-crystal variation of the thermo-optic constants. (3) The Gd or La molar concentration gradient in the mixed crystals. Umemura et al ever measured the 90° phase-matching temperature for type-I third-harmonic-generation at 355 nm by using three y-cut Gd0.32Y0.78OB crystals. Although their index and thermo-optic formulas for YCOB and GdCOB give the 90° phase-matching temperature of Tpm ∇ 109 °C, the experimental values were Tpm ∇ 85 ± 1 °C, 93 ± 1 °C, and 102 ± 1 °C, respectively [44]. This example proved that the temperature characteristics of RECOB crystals do exist large individual difference.

Tables Icon

Table 7. Temperature acceptance bandwidth of NCPM SHG in YCOB and GdCOB crystals

On the whole, the temperature acceptance bandwidth of RECOB crystals are much larger than that of LBO crystal, such property can reduce the requirement of the temperature controlling and is favourable for high stability NLO frequency conversions. As early as 2002, we have confirmed this property by SHG experiments of 1064 nm laser. For this frequency conversion of YCOB and GdCOB crystals, the PM angle which is closest to the optical principle axes is (90°, 75.4°), corresponding to the Type-II PM of YCOB crystal. So it is the most promising angle to achieve NCPM by changing the crystal temperature. Using an extra cavity frequency doubling experiment equipment and a (90°, 90°)-cut (i.e. Y-cut) YCOB sample, we monitored the changing of this PM angle with the crystal temperature. Although this PM angle was indeed gradually close to the Y axis with the increasing of temperature, but the speed was very slow. When the crystal temperature was elevated to 150°C from a room temperature of 20 °C, this PM direction only changed about 6°, and the angular distance from Y-axis was still 9° or so [47]. At the same temperature variation range, the PM angle of LBO crystal will change 12°, and the one of MgO:LiNbO3 crystal will change more than 14°, which have realized A-NCPM SHG [48]. On the PM direction (31°, 180°) of YCOB crystal, the temperature acceptance bandwidth is found to be even larger than 150°C, reported by A. Kausas et al very recently [49].

In the future, as long as the thermo-optic dispersion formula of other RECOB (RE = Sm, Nd, La and Tm) crystals are supplied, according to the Table 10 their temperature acceptance bandwidths can be calculated out and supplemented to the Table 7.

11. Conclusion

As a kind of relatively new NLO material, the excellent comprehensive performance makes RECOB type crystals have many practical applications. The members of RECOB type crystals are numerous. RE3+ ions can be one or more kinds of trivalent rare-earth cations, in addition, Ca2+ ions can be partially replaced by two valent cations [50,51]. The crystal refractive indexes can be adjusted in a large scope by changing the components, correspondingly the PM properties can be changed dramatically. This advantage of RECOB type crystals brings the important NLO application, i.e. the broad waveband tunable NCPM.

In this paper, we intensively investigated the NCPM SHG properties of six RECOB (RE = Tm, Y, Gd, Sm, Nd and La) crystals. Based on the experimental results and the theoretical analysis, we discovered an important discipline that the closer ion radius between RE3+ and Ca2+, the smaller birefringence, and the longer NCPM SHG wavelength, the better angular and wavelength acceptance bandwidths. The analytical formula of the characteristic parameters for NCPM SHG were obtained by theoretical derivations. Referencing the refractive index attributes, the calculation results agreed well with the experimental data. The present research illustrates that RECOB type crystals are potential NCPM SHG materials for various near infrared wavelengths. At the same time, the discipline that we have discovered between the crystal component and the NCPM characteristics will contribute to the design of novel, excellent NCPM materials in the future.

12. Appendix

12.1 A discussion about the relationship between birefringence and NCPM SHG wavelength

(1) Type-I NCPM SHG on Y-axis

For this PM style, the refractive indexes of the NLO crystal should satisfy the condition

nZ(ω)=nX(2ω)
where nz(ω), nx(2ω) are the refractive index on Z-axis for the fundamental wave, on X-axis for the SHG wave, respectively. Combining with the Eq. (A.1.1) in the main text, we can obtain
nZ(ω)2nX(ω)2=nX(2ω)2nX(ω)2
=BX(λ2)2CXDX(λ2)2(BXλ2CXDXλ2)
=3BXλ2(λ24CX)(λ2CX)+34DXλ2
where λ is the wavelength of the fundamental wave when the type-I NCPM SHG is realized. From Table 3, it can be known that for various RECOB type crystals there are Bx = 0.022 ( ± 0.002), Cx = 0.016 ( ± 0.003), Dx = 0.006 ( ± 0.003). From Tables 5 and 6, it can be known that λ is 0.8 ( ± 0.1) μm. Taking these values into the right side of the Eq. (6), the first term and the second term change to 0.1836λ2 and 0.0045λ2, respectively. So the first term is about 40 times of the second term, the second term can be omitted approximately. Since λ2 is also about 40 times of Cx, we can further simplify the coefficient (λ2-Cx) of the first term to be λ2. Considering above approximations, the Eq. (6) can be rewritten as
Δn(ω)=nZ(ω)nX(ω)3BXλ24CX×1nZ(ω)+nX(ω)
From the Sellmeier equation coefficients of Table 3, we can calculate nZ(ω)-nX(ω) and nZ(ω) + nX(ω) at 0.8 μm of these crystals, which are 0.365 ± 0.075, 3.385 ± 0.015, respectively. Comparing with the ± 20.5% variation of nZ(ω)-nX(ω), the ± 0.44% variation of nZ(ω) + nX(ω) is much smaller, which can be regarded as a constant term that is independent with ω or λ. Under this approximation, there is
Δn(ω)=nZ(ω)nX(ω)3BXλ24CX
It indicates that the birefringence Δn and NCPM SHG wavelength λ have approximate inverse relationship, i.e. small birefringence will present long NCPM SHG wavelength.

(2) Type-II NCPM SHG on Y-axis

For this PM style, the refractive indexes of the NLO crystal should satisfy the condition

nZ(ω)+nX(ω)2=nX(2ω)
where nz(ω), nx(ω) are the Z-polarization, X-polarization refractive indexes of the fundamental wave, respectively. From the Eq. (9), we can obtain
(nZ(ω)+nX(ω)2)2nX(ω)2=nX(2ω)2nX(ω)2
Referencing the Eqs. (4) - (7), there is

(nZ(ω)+nX(ω)2)2nX(ω)23BXλ24CX

i.e.

Δn(ω)=nZ(ω)nX(ω)3BXλ24CX×4nZ(ω)+3nX(ω)
Based on the similar analysis as above part, it can be known that the variation of nZ(ω) + 3nX(ω) is relatively small, so it can be recognized as a constant term. Thus, there is
Δn(ω)=nZ(ω)nX(ω)3BXλ24CX
It indicates that in this condition the birefringence Δn and NCPM SHG wavelength λ also have approximate inverse relationship.

(3) Type-I NCPM SHG on Z-axis

For this PM style, the refractive indexes of the NLO crystal should satisfy the condition

nY(ω)=nX(2ω)
Experiencing a similar discussion procedure with that of type-I NCPM SHG on Y-axis, we obtain
Δn(ω)=nY(ω)nX(ω)3BXλ24CX
So for this PM style, the birefringence Δn and NCPM SHG wavelength λ still have inverse relationship.

12.2 Angular acceptance bandwidth of NCPM SHG

When the actual situations deviate from the ideal PM conditions, a mismatch of wave vector Δk will appear, and the SHG conversion efficiencyη can be expressed as

η=η0[sin(Δk2l)Δk2l]2
where η0 is the maximum SHG conversion efficiency under the ideal PM conditions, i.e. Δk = 0, and l is the transmission length of the NLO medium. When Δk = ± π/l, η will decreases to 40% or so of η0, and the corresponding parameter value in Δk is defined as the acceptance of this parameter. It is 13% greater than the full width at half maximum of the sinc2kl/2) function in Eq. (16), which corresponds to a 50% decreasing of η0. Here we firstly consider the situation about the spatial angle θ. Around the PM angle (θm, ϕm), Δk can be expanded to the followed Taylor series about the θ angle
Δk=Δk|(θ=θm,ϕ=ϕm)+Δkθ|(θ=θm,ϕ=ϕm)Δθ+122Δkθ2|(θ=θm,ϕ=ϕm)Δθ2
So the angler acceptance in θ direction, i.e. Δθ, can be theoretically deduced from the Eq. (17) and the definition of Δk = ± π/l, if Δk/θ and 2Δk/θ2 is known. The followed part is a detailed deduction of these two parameters.

For three wave frequency mixing, based on the expression of k = 2πn/λ, there is

Δk=k3k2k1=2πλ3n32πλ2n22πλ1n1
So
Δkθ=2πλ3n(ω3)θ2πλ2n(ω2)θ2πλ1n(ω1)θ
2Δkθ2=2πλ32n(ω3)θ22πλ22n(ω2)θ22πλ1n2(ω1)θ2
It is known that the polarized refractive index of anisotropic crystal on the light transmission direction (θ, ϕ) has the followed form
n(ωi)=(2Bi±Bi24Ci)12i=1,2,3
For type-I PM the sign in above equation is “−” for i = 1, 2 which represents the slow fundamental wave, and the sign is “+” for i = 3 which represents the fast mixing frequency wave. Correspondingly, for type-II PM the sign is “−” for i = 1 which represents the slow fundamental wave, and the sign is “+” for i = 2, 3 which represents the fast fundamental wave and the fast mixing frequency wave, respectively. In the Eq. (21), there is
Bi=sin2θcos2ϕ[ny2(ωi)+nz2(ωi)]sin2θsin2ϕ[nx2(ωi)+nz2(ωi)]cos2θ[nx2(ωi)+nz2(ωi)]
Ci=sin2θcos2ϕny2(ωi)nz2(ωi)+sin2θsin2ϕnx2(ωi)nz2(ωi)+cos2θnx2(ωi)nz2(ωi)
From the Eq. (21), it can be obtained that
niθ=22(Bi±Bi24Ci)32(Biθ±BiBiθ2CiθBi24Ci)
2niθ2=22{(Bi±Bi24Ci)52(32)(Biθ±BiBiθ2CiθBi24Ci)2}22(Bi±Bi24Ci)32{2Biθ2±[((Biθ)2+Bi2Biθ222Ciθ2)1Bi24Ci(BiBiθ2Ciθ)2(Bi24Ci)32]}
where
Biθ=[nx2(ωi)+ny2(ωi)nz2(ωi)cos2ϕny2(ωi)sin2ϕnx2(ωi)]sin2θ
2Biθ2=[nx2(ωi)+ny2(ωi)nz2(ωi)cos2ϕny2(ωi)sin2ϕnx2(ωi)]2cos2θ
Ciθ=[ny2(ωi)nz2(ωi)cos2ϕ+nx2(ωi)nz2(ωi)sin2ϕnx2(ωi)ny2(ωi)]sin2θ
2Ciθ2=[ny2(ωi)nz2(ωi)cos2ϕ+nx2(ωi)nz2(ωi)sin2ϕnx2(ωi)ny2(ωi)]2cos2θ
At NCPM conditions there is θ = θm = 0° or 90°, so Bi/θ and Ci/θ will be zero because the Eqs. (26) and (28) contain the term of “sin2θ”. So ni/θ and Δk/θ will be zero from the Eqs. (24) and (19), respectively. Simultaneously considering Δk|(θ=θm,φ=φm)=0 at angular PM conditions, the right side of the Eq. (17) will only left the third term, and the angler acceptance Δθ can be obtained from the followed formula
Δk=122Δkθ2|(θ=θm,φ=φm)Δθ2=±πl
i.e. the angler acceptance bandwidth in θ direction for NCPM can be expressed as
Δθl12=[4π/2Δkθ2|(θ=θm,φ=φm)]12
where 2Δk/θ2 can be obtained from the Eqs. (20), (25), (27) and (29). For example, to the type-I NCPM on Y-axis of biaxial crystal, i.e. (θm = 90°, ϕm = 90°), there is
2niθ2=2[nx2(ωi)+nz2(ωi)±(nx2(ωi)nz2(ωi))]32[ny2(ωi)nz2(ωi)±(nz2(ωi)ny2(ωi))]
At SHG condition (ω1 = ω2), according to the sign selection rules mentioned above, we can get
2n1θ2=2n2θ2=nz3(ω1)(ny2(ω1)nz2(ω1))i=1,2
2n3θ2=0i=3
So the angular acceptance bandwidth in θ direction for such NCPM SHG configuration can be deduced from the Eqs. (20) and (31), which is
Δθl12=10λ12nz3(ω1)(ny2(ω1)nz2(ω1))(mradcm12)
Similarly, the angular acceptance bandwidth in θ direction for other five kinds of NCPM SHG configurations can be deduced out, which are listed in the Table 8.

Tables Icon

Table 8. Angular acceptance bandwidth of NCPM SHG in biaxial NLO crystal

Based on the similar deduction procedures, we obtain the angular acceptance bandwidth in ϕ direction for all of the six kinds of NCPM SHG configurations, and list them in Table 8 as well. For the NCPM on Z axis (θ = 0), the change of spatial direction is only related to the parameter θ, so the angular acceptance bandwidths on the two principal planes, XZ and YZ, are both recorded as Δθl1/2, which are distinguished by PM angles, i.e. (0°, 0°), (0°, 90°), respectively. It can be seen that on the same principal axis the angular acceptance bandwidth of type-II NCPM is usually larger than that of type-I NCPM, which exhibits a 2 times increase.

12.3 Wavelength acceptance bandwidth of NCPM SHG

For three wave frequency mixing, the three wavelengths satisfy the followed formula

1λ1+1λ2=1λ3
If the fundamental wavelengths have the offsets Δλ1 and Δλ2, the above formula will be
1λ1+Δλ1+1λ2+Δλ2=1λ3+Δλ3
i.e.
Δλ3=(λ1+Δλ1)(λ2+Δλ2)λ1+Δλ1+λ2+Δλ2λ3
For SHG, a special case of three wave frequency mixing, there is λ1 = λ2, so λ3 = λ1/2 from the Eq. (36), and Δλ3 = Δλ1/2 from the Eq. (38).

Around the central PM wavelength λ10, the mismatch of wave vector Δk can be expressed as the followed Taylor series about the wavelength λ1

Δk=Δk|λ1=λ10+Δkλ1|λ1=λ10Δλ1+122Δkλ12|λ1=λ10(Δλ1)2+
At the central PM wavelength λ10, there is Δk|λ1=λ10=0. To the angular NCPM concerned in this paper, the parameter Δk/λ1 is usually not equal to zero, so we can solely reserve this term and ignore the higher order derivative terms, for the convenience of the calculation. Thus,
Δk=Δkλ1|λ1=λ10Δλ1
Based on the expression of wave vector, i.e. k = 2πn/λ, there is
Δk=K3K2K1=2πλ3n32πλ2n22πλ1n1
So
Δkλ1=2π{[n3λ1λ3+n3(1λ32λ3λ1)][n2λ1λ2+n2(1λ22λ2λ1)][n1λ1λ1+n1(1λ12λ1λ1)]}
Considering λ1 = λ2 and λ3 = λ1/2, there are λ3/λ1=1/2, λ2/λ1=1, and λ1/λ1=1. So the Eq. (42) can be simplified as
Δkλ1=2π(2n3λ1n2λ1n1λ1λ12n3n2n1λ12)
At the PM condition λ = λ10, there is 2n3 = n2 + n1, so
Δkλ1=2πλ1(2n3λ1n2λ1n1λ1)
Because we only consider the angular NCPM styles in this paper, all of n3, n2, and n1 are principal refractive indexes. The principal refractive indexes of biaxial crystal are
nj2(ωi)=Aj+Bjλi2CjDjλi2j=X,Y,Zi=1,2,3
So nj(ωi)/λ1 can be derived as
nj(ωi)λ1=Bj(λi2Cj)2DjAj+Bjλi2CjDjλi2λiλiλ1
where λ3/λ1=1/2, λ2/λ1=1, and λ1/λ1=1.

Considering the equation (40) and the definition of the wavelength acceptance bandwidth, we can obtain

Δk=Δkλ1|λ1=λ10Δλ1=±πl
i.e.
Δλ1l=2π|(Δkλ1|λ1=λ10)1|
where Δkλ1|λ1=λ10 can be obtained from the Eqs. (44) and (46).

Below we will discuss the type-I NCPM SHG on Y-axis of biaxial crystal as an example. From the Eq. (46), there is

nZ(ω1)λ1=nZ(ω2)λ1=BZ(λ12CZ)2DZAZ+BZλ12CZDZλ12λ1
nX(ω3)λ1=BX(λ32CX)2DXAX+BXλ32CXDXλ32(λ32)
For type-I NCPM SHG, n3 = nX3), n2 = n1 = nZ1) in the Eq. (44). Taking Eq. (49) and (50) into the Eq. (44), we can achieve
Δkλ1=2πλ1(BX(λ32CX)2DXAX+BXλ32CXDXλ32λ32BZ(λ12CZ)2DZAZ+BZλ12CZDZλ12λ1)
=2πλ1(BX(λ32CX)2DXnX(ω3)λ32BZ(λ12CZ)2DZnZ(ω1)λ1)
=π[4BZ(λ12CZ)2+DZnZ(ω1)BX(λ32CX)2+DXnX(ω3)]
Taking Eq. (51) into the Eq. (48), the wavelength acceptance bandwidth of type-I NCPM SHG is obtained to be
Δλ1l=2|[4BZ(λ12CZ)2+DZnZ(ω1)BX(λ32CX)2+DXnX(ω3)]1|λ1=λ10|
=2|[4BZ(λ102CZ)2+DZnZ(ω10)16BX(λ1024CX)2+DXnX(ω30)]1|
=2|[4BZ(λ102CZ)2+4DZ16BX(λ1024CX)2DXnZ(λ10)]1|
Similarly, the wavelength acceptance bandwidth for other five kinds of NCPM SHG configurations can also be deduced out, which are listed in the Table 9.

Tables Icon

Table 9. Wavelength acceptance bandwidth of NCPM SHG in biaxial NLO crystal

12.4 Temperature acceptance bandwidth of NCPM SHG

The variations of the principal refractive indexes with the temperature can be expressed by

nX(λ)=n0X(λ)+nX(λ)TΔT
nY(λ)=n0Y(λ)+nY(λ)TΔT
nZ(λ)=n0Z(λ)+nZ(λ)TΔT
where n0X(λ), n0Y(λ), and n0Z(λ) are the principal refractive indexes at normal atmospheric temperature T0. The wave vector mismatching for three wave frequency mixing is
Δk=k3k2k1=2πλ3n32πλ2n22πλ1n1
So, its first order derivative with respect to temperature is given by
ΔkT=2πλ3n3T2πλ2n2T2πλ1n1T
For SHG where λ1 = λ2, λ3 = λ1/2, there is
ΔkT=2πλ1(2n3Tn2Tn1T)
The mismatch of wave vector Δk can be expressed as the followed expression about the temperature
Δk=ΔkT|T=T0ΔT
Considering the definition of the temperature acceptance bandwidth (Δk = ± π/l), we can obtain
ΔTl=2π|(ΔkT|T=T0)1|
=λ12n3Tn2Tn1T
For the angular NCPM SHG considered in this paper, all of n3, n2, and n1 are principal refractive indexes. So n3T, n2T, and n1T are the principal refractive index−temperature coefficients, as demonstrated in the Eqs. (53)-(55).

For the type-I angular NCPM SHG on Y-axis of biaxial crystal, there are n3 = nX3), n1 = n2 = nZ1). From the Eq. (60), the temperature acceptance bandwidth at this situation is obtained to be

ΔTl=λ12[nX(λ3)TnZ(λ1)T]
Similarly, the temperature acceptance bandwidth for other five kinds of angular NCPM SHG configurations can also be deduced out, which are listed in the Table 10.

Tables Icon

Table 10. Temperature acceptance bandwidth of NCPM SHG in biaxial NLO crystals

13. Funding

National Natural Science Foundation of China (NSFC) (Grant Nos. 61178060, 51202129 and 91022034); Nature Science Foundation of Shandong Province (ZR2012EMQ004); Natural Science Foundation for Distinguished Young Scholar of Shandong Province (2012JQ18).

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Figures (7)

Fig. 1
Fig. 1 As-grown RECOB crystals (RE = Tm, Y, Gd, Sm, Nd and La).
Fig. 2
Fig. 2 Transmission spectra of several colored RECOB crystals.
Fig. 3
Fig. 3 Relationships between the crystallographic axes (a, b and c) and the optical principal axes (X, Y and Z) for RECOB crystals.
Fig. 4
Fig. 4 Refractive-index dispersion curves of several RECOB crystals.
Fig. 5
Fig. 5 Variation of birefringence and NCPM SHG wavelength with rare earth ion radius in RECOB crystals.
Fig. 6
Fig. 6 External angular tuning curves of the SHG signals in different RECOB crystals, for the type-I NCPM on Y axis.
Fig. 7
Fig. 7 Wavelength tuning curves of the SHG signals in different RECOB crystals, for the type-I SHG on Y axis.

Tables (10)

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Table 1 Crystal orientation of RECOB crystals

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Table 2 Sellmeier equation coefficients of RECOB crystals

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Table 3 The effective nonlinear optical coefficients deff of RECOB type crystals along different optical principal axes. The values of the NLO coefficients came from Reference [37].

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Table 4 Calculated and measured NCPM SHG wavelength of RECOB crystals

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Table 5 External angular acceptance bandwidth of NCPM SHG in RECOB crystals

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Table 6 Wavelength acceptance bandwidth of NCPM SHG in different RECOB crystals

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Table 7 Temperature acceptance bandwidth of NCPM SHG in YCOB and GdCOB crystals

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Table 8 Angular acceptance bandwidth of NCPM SHG in biaxial NLO crystal

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Table 9 Wavelength acceptance bandwidth of NCPM SHG in biaxial NLO crystal

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Table 10 Temperature acceptance bandwidth of NCPM SHG in biaxial NLO crystals

Equations (66)

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n i 2 = A i + B i λ 2 C i D i λ 2 (i=X,Y,Z)
d 11 d 12 d 13 0 0 0 d 31 d 32 d 33 0 d 31 0 d 32 0 d 12 0 d 13 0
n Z (ω)= n X (2ω)
n Z (ω) 2 n X (ω) 2 = n X (2ω) 2 n X (ω) 2
= B X ( λ 2 ) 2 C X D X ( λ 2 ) 2 ( B X λ 2 C X D X λ 2 )
= 3 B X λ 2 ( λ 2 4 C X )( λ 2 C X ) + 3 4 D X λ 2
Δn(ω)= n Z (ω) n X (ω) 3 B X λ 2 4 C X × 1 n Z (ω)+ n X (ω)
Δn(ω)= n Z (ω) n X (ω) 3 B X λ 2 4 C X
n Z (ω)+ n X (ω) 2 = n X (2ω)
( n Z (ω)+ n X (ω) 2 ) 2 n X (ω) 2 = n X (2ω) 2 n X (ω) 2
( n Z (ω)+ n X (ω) 2 ) 2 n X (ω) 2 3 B X λ 2 4 C X
Δn(ω)= n Z (ω) n X (ω) 3 B X λ 2 4 C X × 4 n Z (ω)+3 n X (ω)
Δn(ω)= n Z (ω) n X (ω) 3 B X λ 2 4 C X
n Y (ω)= n X (2ω)
Δn(ω)= n Y (ω) n X (ω) 3 B X λ 2 4 C X
η= η 0 [ sin( Δk 2 l ) Δk 2 l ] 2
Δk=Δk| ( θ= θ m ,ϕ= ϕ m ) + Δk θ | ( θ= θ m ,ϕ= ϕ m ) Δθ+ 1 2 2 Δk θ 2 | ( θ= θ m ,ϕ= ϕ m ) Δ θ 2
Δk= k 3 k 2 k 1 = 2π λ 3 n 3 2π λ 2 n 2 2π λ 1 n 1
Δk θ = 2π λ 3 n( ω 3 ) θ 2π λ 2 n( ω 2 ) θ 2π λ 1 n( ω 1 ) θ
2 Δk θ 2 = 2π λ 3 2 n( ω 3 ) θ 2 2π λ 2 2 n( ω 2 ) θ 2 2π λ 1 n 2 ( ω 1 ) θ 2
n( ω i )= ( 2 B i ± B i 2 4 C i ) 1 2 i=1,2,3
B i = sin 2 θ cos 2 ϕ[ n y 2 ( ω i )+ n z 2 ( ω i ) ] sin 2 θ sin 2 ϕ[ n x 2 ( ω i )+ n z 2 ( ω i ) ] cos 2 θ[ n x 2 ( ω i )+ n z 2 ( ω i ) ]
C i = sin 2 θ cos 2 ϕ n y 2 ( ω i ) n z 2 ( ω i )+ sin 2 θ sin 2 ϕ n x 2 ( ω i ) n z 2 ( ω i ) + cos 2 θ n x 2 ( ω i ) n z 2 ( ω i )
n i θ = 2 2 ( B i ± B i 2 4 C i ) 3 2 ( B i θ ± B i B i θ 2 C i θ B i 2 4 C i )
2 n i θ 2 = 2 2 { ( B i ± B i 2 4 C i ) 5 2 ( 3 2 ) ( B i θ ± B i B i θ 2 C i θ B i 2 4 C i ) 2 } 2 2 ( B i ± B i 2 4 C i ) 3 2 { 2 B i θ 2 ±[ ( ( B i θ ) 2 + B i 2 B i θ 2 2 2 C i θ 2 ) 1 B i 2 4 C i ( B i B i θ 2 C i θ ) 2 ( B i 2 4 C i ) 3 2 ] }
B i θ =[ n x 2 ( ω i )+ n y 2 ( ω i ) n z 2 ( ω i ) cos 2 ϕ n y 2 ( ω i ) sin 2 ϕ n x 2 ( ω i ) ]sin2θ
2 B i θ 2 =[ n x 2 ( ω i )+ n y 2 ( ω i ) n z 2 ( ω i ) cos 2 ϕ n y 2 ( ω i ) sin 2 ϕ n x 2 ( ω i ) ]2cos2θ
C i θ =[ n y 2 ( ω i ) n z 2 ( ω i ) cos 2 ϕ+ n x 2 ( ω i ) n z 2 ( ω i ) sin 2 ϕ n x 2 ( ω i ) n y 2 ( ω i ) ]sin2θ
2 C i θ 2 =[ n y 2 ( ω i ) n z 2 ( ω i ) cos 2 ϕ+ n x 2 ( ω i ) n z 2 ( ω i ) sin 2 ϕ n x 2 ( ω i ) n y 2 ( ω i ) ]2cos2θ
Δk= 1 2 2 Δk θ 2 | (θ= θ m ,φ= φ m ) Δ θ 2 =± π l
Δθ l 1 2 = [ 4π/ 2 Δk θ 2 | (θ= θ m ,φ= φ m ) ] 1 2
2 n i θ 2 = 2 [ n x 2 ( ω i )+ n z 2 ( ω i )±( n x 2 ( ω i ) n z 2 ( ω i ) ) ] 3 2 [ n y 2 ( ω i ) n z 2 ( ω i )±( n z 2 ( ω i ) n y 2 ( ω i ) ) ]
2 n 1 θ 2 = 2 n 2 θ 2 = n z 3 ( ω 1 )( n y 2 ( ω 1 ) n z 2 ( ω 1 ) )i=1,2
2 n 3 θ 2 =0 i= 3
Δθ l 1 2 =10 λ 1 2 n z 3 ( ω 1 )( n y 2 ( ω 1 ) n z 2 ( ω 1 )) (mradc m 1 2 )
1 λ 1 + 1 λ 2 = 1 λ 3
1 λ 1 +Δ λ 1 + 1 λ 2 +Δ λ 2 = 1 λ 3 +Δ λ 3
Δ λ 3 = ( λ 1 +Δ λ 1 )( λ 2 +Δ λ 2 ) λ 1 +Δ λ 1 + λ 2 +Δ λ 2 λ 3
Δk=Δk| λ 1 = λ 10 + Δk λ 1 | λ 1 = λ 10 Δ λ 1 + 1 2 2 Δk λ 1 2 | λ 1 = λ 10 (Δ λ 1) 2 +
Δk= Δk λ 1 | λ 1 = λ 10 Δ λ 1
Δk= K 3 K 2 K 1 = 2π λ 3 n 3 2π λ 2 n 2 2π λ 1 n 1
Δk λ 1 =2π{ [ n 3 λ 1 λ 3 + n 3 ( 1 λ 3 2 λ 3 λ 1 ) ][ n 2 λ 1 λ 2 + n 2 ( 1 λ 2 2 λ 2 λ 1 ) ][ n 1 λ 1 λ 1 + n 1 ( 1 λ 1 2 λ 1 λ 1 ) ] }
Δk λ 1 =2π( 2 n 3 λ 1 n 2 λ 1 n 1 λ 1 λ 1 2 n 3 n 2 n 1 λ 1 2 )
Δk λ 1 = 2π λ 1 ( 2 n 3 λ 1 n 2 λ 1 n 1 λ 1 )
n j 2 ( ω i )= A j + B j λ i 2 C j D j λ i 2 j=X,Y,Z i=1,2,3
n j ( ω i ) λ 1 = B j ( λ i 2 C j ) 2 D j A j + B j λ i 2 C j D j λ i 2 λ i λ i λ 1
Δk= Δk λ 1 | λ 1 = λ 10 Δ λ 1 =± π l
Δ λ 1 l=2π| ( Δk λ 1 | λ 1 = λ 10 ) 1 |
n Z ( ω 1 ) λ 1 = n Z ( ω 2 ) λ 1 = B Z ( λ 1 2 C Z ) 2 D Z A Z + B Z λ 1 2 C Z D Z λ 1 2 λ 1
n X ( ω 3 ) λ 1 = B X ( λ 3 2 C X ) 2 D X A X + B X λ 3 2 C X D X λ 3 2 ( λ 3 2 )
Δk λ 1 = 2π λ 1 ( B X ( λ 3 2 C X ) 2 D X A X + B X λ 3 2 C X D X λ 3 2 λ 3 2 B Z ( λ 1 2 C Z ) 2 D Z A Z + B Z λ 1 2 C Z D Z λ 1 2 λ 1 )
= 2π λ 1 ( B X ( λ 3 2 C X ) 2 D X n X ( ω 3 ) λ 3 2 B Z ( λ 1 2 C Z ) 2 D Z n Z ( ω 1 ) λ 1 )
=π[4 B Z ( λ 1 2 C Z ) 2 + D Z n Z ( ω 1 ) B X ( λ 3 2 C X ) 2 + D X n X ( ω 3 ) ]
Δ λ 1 l=2| [4 B Z ( λ 1 2 C Z ) 2 + D Z n Z ( ω 1 ) B X ( λ 3 2 C X ) 2 + D X n X ( ω 3 ) ] 1 | λ 1 = λ 10 |
=2| [4 B Z ( λ 10 2 C Z ) 2 + D Z n Z ( ω 10 ) 16 B X ( λ 10 2 4 C X ) 2 + D X n X ( ω 30 ) ] 1 |
=2| [ 4 B Z ( λ 10 2 C Z ) 2 +4 D Z 16 B X ( λ 10 2 4 C X ) 2 D X n Z ( λ 10 ) ] 1 |
n X (λ)= n 0X (λ)+ n X (λ) T ΔT
n Y (λ)= n 0Y (λ)+ n Y (λ) T ΔT
n Z (λ)= n 0Z (λ)+ n Z (λ) T ΔT
Δk= k 3 k 2 k 1 = 2π λ 3 n 3 2π λ 2 n 2 2π λ 1 n 1
Δk T = 2π λ 3 n 3 T 2π λ 2 n 2 T 2π λ 1 n 1 T
Δk T = 2π λ 1 (2 n 3 T n 2 T n 1 T )
Δk= Δk T | T= T 0 ΔT
ΔTl=2π| ( Δk T | T= T 0 ) 1 |
= λ 1 2 n 3 T n 2 T n 1 T
ΔTl= λ 1 2[ n X ( λ 3 ) T n Z ( λ 1 ) T ]
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